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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654014Generated: October 26, 2026

4-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzoic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethyl-amide] → 4-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzoic acid-(2,3,4-trihydroxy-butyl)-amide

https://huagongshe.com/reaction/654014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzoic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethyl-amide]HCID 15057608—
SolventMethanol--water (1/1)HCID 22242641—
Product4-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzoic acid-(2,3,4-trihydroxy-butyl)-amideHCID 15057609—

Reaction Steps

2.53 g (5 mmol) of 4-[N-(4-fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzoic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamide] is dissolved in 20 ml of methanol/water 1:1, about 100 mg of cation exchanger Amberlyst 15 is added and warmed for 1 hour to boiling temperature. The ion exchanger is then filtered off and the filtrate is evaporated to dryness in a vacuum. 1.74 g (3.75 mmol)=75% of the theoretical yield of the product is obtained as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05130119
Source datasetuspto-grants-1992_07
ORD IDord-4f5905b2d21a491c949312d317ca9b9e
Source noteuspto-grants-1992_07